Congenital hypothyroidism medical therapy: Difference between revisions

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==Overview==
==Overview==
==Medical Therapy==
==Medical Therapy==
The goal of newborn [[screening]] programs is to detect and start treatment within the first 1-2 weeks of life. Treatment consists of a daily dose of [[thyroxine]], available as a small tablet. The generic name is [[levothyroxine]], and several brands are available. Commonly used brands in North America are Synthroid, Levoxyl, Unithroid, and Levothroid. The tablet is crushed and given to the infant with a small amount of water or milk. The most commonly recommended dose range is 10-15 μg/kg daily, typically 37.5 or 44 μg.<ref>Journal of Pediatric Endocinology and Metabolism 20:559 '''PMID 17642417'''</ref>
The goal of newborn [[screening]] programs is to detect and start treatment within the first 1-2 weeks of life. Treatment consists of a daily dose of [[thyroxine]], available as a small tablet. The generic name is [[levothyroxine]], and several brands are available. Commonly used brands in North America are Synthroid, Levoxyl, Unithroid, and Levothroid. The tablet is crushed and given to the infant with a small amount of water or milk. The most commonly recommended dose range is 10-15 μg/kg daily, typically 37.5 or 44 μg.<ref>Journal of Pediatric Endocinology and Metabolism 20:559 '''PMID 17642417'''</ref>


Within a few weeks, the T<sub>4</sub> and TSH levels are rechecked to confirm that they are being normalized by treatment. As the child grows up, these levels are checked regularly to maintain the right dose. The dose increases as the child grows.
Within a few weeks, the T<sub>4</sub> and TSH levels are rechecked to confirm that they are being normalized by treatment. As the child grows up, these levels are checked regularly to maintain the right dose. The dose increases as the child grows.
==References==
==References==
{{reflist|2}}
{{reflist|2}}
{{WH}}
 
{{WS}}
[[Category:Congenital disorders]]
[[Category:Endocrinology]]
[[Category:Endocrinology]]
[[Category:Disease]]
[[Category:Disease]]
[[Category:Neonatology]]
 
[[Category:Mature chapter]]
{{WS}}
{{WH}}

Latest revision as of 16:08, 22 July 2016

Congenital hypothyroidism Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Congenital hypothyroidism from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X Ray

CT

MRI

Ultrasound

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

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Most cited articles

Review articles

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X-rays
Echo & Ultrasound
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MRI

Ongoing Trials at Clinical Trials.gov

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NICE Guidance

FDA on Congenital hypothyroidism medical therapy

CDC on Congenital hypothyroidism medical therapy

Congenital hypothyroidism medical therapy in the news

Blogs on Congenital hypothyroidism medical therapy

Directions to Hospitals Treating Congenital hypothyroidism

Risk calculators and risk factors for Congenital hypothyroidism medical therapy

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:

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Overview

Medical Therapy

The goal of newborn screening programs is to detect and start treatment within the first 1-2 weeks of life. Treatment consists of a daily dose of thyroxine, available as a small tablet. The generic name is levothyroxine, and several brands are available. Commonly used brands in North America are Synthroid, Levoxyl, Unithroid, and Levothroid. The tablet is crushed and given to the infant with a small amount of water or milk. The most commonly recommended dose range is 10-15 μg/kg daily, typically 37.5 or 44 μg.[1]

Within a few weeks, the T4 and TSH levels are rechecked to confirm that they are being normalized by treatment. As the child grows up, these levels are checked regularly to maintain the right dose. The dose increases as the child grows.

References

  1. Journal of Pediatric Endocinology and Metabolism 20:559 PMID 17642417

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